Abiusi, Emanuela
 Distribuzione geografica
Continente #
EU - Europa 461
NA - Nord America 387
AS - Asia 221
AF - Africa 10
SA - Sud America 1
Totale 1.080
Nazione #
US - Stati Uniti d'America 380
SE - Svezia 149
IT - Italia 109
DE - Germania 73
CN - Cina 72
SG - Singapore 63
TR - Turchia 32
IE - Irlanda 31
ID - Indonesia 21
RU - Federazione Russa 20
UA - Ucraina 15
FI - Finlandia 13
FR - Francia 12
IR - Iran 11
CI - Costa d'Avorio 10
GB - Regno Unito 10
NL - Olanda 9
IN - India 7
HK - Hong Kong 6
KR - Corea 5
CZ - Repubblica Ceca 4
CA - Canada 3
CH - Svizzera 3
AT - Austria 2
BE - Belgio 2
CR - Costa Rica 2
LT - Lituania 2
PK - Pakistan 2
BA - Bosnia-Erzegovina 1
BR - Brasile 1
ES - Italia 1
HR - Croazia 1
IL - Israele 1
LI - Liechtenstein 1
MD - Moldavia 1
MX - Messico 1
NO - Norvegia 1
PA - Panama 1
RS - Serbia 1
VN - Vietnam 1
Totale 1.080
Città #
Chandler 93
Ashburn 44
Singapore 44
Dublin 29
Milan 27
New York 24
Jakarta 21
Rome 18
San Mateo 14
Nanchang 12
Izmir 11
Munich 11
Abidjan 10
Jacksonville 10
Nanjing 10
Boston 9
Cattolica 9
Houston 9
Marseille 9
Wilmington 9
Helsinki 7
Princeton 7
Hong Kong 6
Norwalk 6
Old Bridge 6
Bremen 5
Dearborn 5
Fairfield 5
Seoul 5
Shenyang 5
Augusta 4
Beijing 4
Brno 4
Fremont 4
Los Angeles 4
Naaldwijk 4
Nürnberg 4
Seattle 4
Alcamo 3
Amsterdam 3
Boardman 3
Caorle 3
Hefei 3
Lawrence 3
Moscow 3
Redwood City 3
Salò 3
Tehran 3
Tianjin 3
Trivandrum 3
University Park 3
Woodbridge 3
Zurich 3
Ann Arbor 2
Bologna 2
Brixen 2
Brussels 2
Cagliari 2
Cambridge 2
Cesena 2
Changsha 2
Ciserano 2
Cornate d'Adda 2
Hebei 2
Jinan 2
Kish 2
La Cruz 2
Lappeenranta 2
Naples 2
Pisa 2
Taizhou 2
Toronto 2
Turin 2
Vienna 2
Andover 1
Atlanta 1
Aversa 1
Buffalo 1
Busto Arsizio 1
Changchun 1
Chisinau 1
Costa Mesa 1
Council Bluffs 1
Dallas 1
Edinburgh 1
Forest City 1
Frankfurt am Main 1
Fuzhou 1
Groningen 1
Guangzhou 1
Hangzhou 1
Hanoi 1
Juarez 1
Kocaeli 1
Kragujevac 1
Kunming 1
Leipzig 1
Lenoir 1
London 1
Madrid 1
Totale 625
Nome #
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study Running title: adult SMA biomarker study 151
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 92
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: Clues from a biomarker study 86
Neurological assessment of newborns with spinal muscular atrophy identified through neonatal screening 78
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol 73
Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy 69
SMA-miRs (MiR-181a- 5p, -324-5p, and -451a) are overexpressed in spinal muscular atrophy skeletal muscle and serum samples 69
Experience of a 2-year spinal muscular atrophy NBS pilot study in Italy: towards specific guidelines and standard operating procedures for the molecular diagnosis 68
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. 67
Longitudinal assessments in discordant twins with SMA 65
SMA-miRs (MiR-181a- 5p, -324-5p, and -451a) are overexpressed in spinal muscular atrophy skeletal muscle and serum samples 61
Plasma miR-151-3p as a candidate diagnostic biomarker for head and neck cancer: a cross-sectional study within the INHANCE consortium 55
Experience of a 2-year spinal muscular atrophy NBS pilot study in Italy: Towards specific guidelines and standard operating procedures for the molecular diagnosis 30
Early neurological signs in infants identified through neonatal screening for SMA: do they predict outcome? 26
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series 26
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death 18
270th ENMC International Workshop: Consensus for SMN2 genetic analysis in SMA patients 10-12 March, 2023, Hoofddorp, the Netherlands 17
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome 17
Biallelic mutation of UNC50, encoding a protein involved in AChR trafficking, is responsible for arthrogryposis 15
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene 15
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita 13
Totale 1.111
Categoria #
all - tutte 6.569
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.569


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202038 0 0 0 0 4 5 15 2 3 1 5 3
2020/202135 0 3 0 4 4 1 9 1 5 4 4 0
2021/2022130 7 3 7 14 6 5 0 17 10 6 24 31
2022/2023330 56 42 13 30 36 21 39 37 28 7 14 7
2023/2024297 8 50 7 19 15 37 37 3 1 20 42 58
2024/2025119 23 6 34 23 33 0 0 0 0 0 0 0
Totale 1.111